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Monocytic TLR4 expression and activation in schizophrenia: A systematic review and meta-analysis.

作者信息

Jameie Melika, Bordbar Sanaz, Samiee Reza, Amanollahi Mobina, Azizmohammad Looha Mehdi, Aleyasin Mir Sajjad, Abdol Homayuni Mohammad Reza, Mozafar Mehrdad, Jameie Seyed Behnamedin, Akhondzadeh Shahin

机构信息

Neuroscience Research Center, Iran University of Medical Sciences, Tehran, Iran.

Iranian Center of Neurological Research, Neuroscience Institute, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

PLoS One. 2025 Mar 28;20(3):e0319171. doi: 10.1371/journal.pone.0319171. eCollection 2025.


DOI:10.1371/journal.pone.0319171
PMID:40153412
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11952227/
Abstract

BACKGROUND: The role of toll-like receptor 4 (TLR4) in schizophrenia remains unclear, with studies reporting conflicting results on its expression and activation in persons with schizophrenia (PwSCZ). This systematic review/meta-analysis compared basal monocytic TLR4 expression, as well as its activation pattern between PwSCZ and healthy controls (HCs). METHODS: This study was registered with PROSPERO (CRD42021273858) and adhered to the PRISMA guidelines. A systematic search was conducted through MEDLINE (via PubMed), Web of Science, and Scopus from inception to December 12, 2023. Quantitative syntheses were conducted for (a) basal monocytic TLR4 density, (b) basal percentage of TLR4+ monocytes, and (c) basal TLR4 gene expression. Effect sizes were computed using Hedges' g for mean differences. Random-effect models with restricted maximum-likelihood estimation were used, and subgrouping was conducted based on antipsychotic status. The studies' risk of bias was assessed using the Joanna Briggs Institute (JBI) tool. RESULTS: Eleven studies (473 PwSCZ, 416 HCs) were included. Pooled analysis revealed a nonsignificant trend toward increased basal monocytic TLR4 density in PwSCZ (Hedges' g = 0.317 [95% CI: -0.060, 0.694], τ2 = 0.127, I2 = 68.91%). The difference became significant after sensitivity analysis and excluding one study (Hedges' g = 0.469 [0.195,0.742], p = 0.001). No significant difference was found between the groups in terms of TLR4+ monocytes percentage (Hedges' g = 0.235 [-0.245, 0.715], τ2 = 0.31, I2 = 87.30%) or TLR4 gene expression (Hedges' g = 0.179 [-0.502, 0.861], τ2 = 0.29, I2 = 79.04%). According to qualitative synthesis, TLR4 stimulation resulted in reduced monocytic activation in PwSCZ compared to HCs. CONCLUSIONS: This study suggested a trend toward an increased basal monocytic TLR4 density in PwSCZ, with no difference in the basal percentage of TLR4+ monocytes or TLR4 gene expression. However, the limited available data underscores the need for future studies.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf05/11952227/9d6630b592a7/pone.0319171.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf05/11952227/ca828545e880/pone.0319171.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf05/11952227/03db8fe11df8/pone.0319171.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf05/11952227/9d6630b592a7/pone.0319171.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf05/11952227/ca828545e880/pone.0319171.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf05/11952227/03db8fe11df8/pone.0319171.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bf05/11952227/9d6630b592a7/pone.0319171.g003.jpg

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引用本文的文献

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本文引用的文献

[1]
Toll-Like Receptor mRNA Levels in Schizophrenia: Association With Complement Factors and Cingulate Gyrus Cortical Thinning.

Schizophr Bull. 2024-3-7

[2]
Toll-like receptor 4 (TLR4): new insight immune and aging.

Immun Ageing. 2023-11-24

[3]
Immunomodulatory interventions for focal epilepsy.

Cochrane Database Syst Rev. 2023-10-16

[4]
Increased proportions of circulating pro-inflammatory monocytes and macrophages expressing toll-like receptor 4 in individuals with schizophrenia and bipolar disorder receiving medication.

Psychiatry Clin Neurosci. 2023-12

[5]
Incidence, prevalence, and global burden of schizophrenia - data, with critical appraisal, from the Global Burden of Disease (GBD) 2019.

Mol Psychiatry. 2023-12

[6]
Efficacy and safety of adjunctive therapy with fingolimod in patients with schizophrenia: A randomized, double-blind, placebo-controlled clinical trial.

Schizophr Res. 2023-4

[7]
Anti-inflammatory effects of 2nd generation antipsychotics in patients with schizophrenia: A systematic review and meta-analysis.

J Psychiatr Res. 2023-4

[8]
The Dialogue Between Neuroinflammation and Adult Neurogenesis: Mechanisms Involved and Alterations in Neurological Diseases.

Mol Neurobiol. 2023-2

[9]
The relationship between TLR4/NF-κB/IL-1β signaling, cognitive impairment, and white-matter integrity in patients with stable chronic schizophrenia.

Front Psychiatry. 2022-8-16

[10]
Small Study Effects in Diagnostic Imaging Accuracy: A Meta-Analysis.

JAMA Netw Open. 2022-8-1

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